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临床试验/NL-OMON54037
NL-OMON54037招募中不适用

Identification and characterization of non-alcoholic fatty liver disease in primary care. - NAFLD primary care

niversiteit Maastricht0 个研究点目标入组 1,468 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
1,468

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • Able to understand and sign the informed consent
  • Able to speak Dutch
  • Between 18-80 years
  • BMI >25 kg/m²
  • Having one of the following conditions: 1)overweight, 2) obesity, 3) type 2
  • diabetes mellitus, 4) cardiovascular diseases (hypertension, atherosclerosis,
  • angina pectoris, ischaemic heart condition, cerebrovascular condition)
  • Additional inclusion criteria valid only for the other food additives and
  • limonene breath test
  • All those listed in the main protocol +
  • NAFLD F2-F3-F4 fibrosis stage (FibroScan >= 7.5 kPa)
  • Capability to complete an overnight fasting (>=10h)
  • Willingness to share data with Owlstone Medical LTD.

排除标准

  • Excessive alcohol use
  • o more than 20 g/day for women and 30g/day for men
  • o >2 glasses alcohol/day for women and >3 glasses for men
  • Other liver diseases: Hepatitis B virus, Hepatitis C virus, autoimmune
  • hepatitis, primary biliary cirrhosis, hemochromatosis, Wilson*s disease, Alpha
  • 1 antitrypsin deficiency
  • Secondary causes for steatosis: disorders of lipid metabolism, HCV Genotype 3,
  • total parental nutrition, severe surgical weight loss, medications (amiodarone,
  • tamoxifen, methotrexate, corticosteroids and HAART), lean steatosis, Celiac
  • disease, environmental toxicity
  • Pregnancy and breastfeeding.
  • A history of bariatric surgery.
  • Diagnosis of liver cirrhosis and/or hepatocellular carcinoma.
  • Current diagnosis of extrahepatic malignancy(s) or prior diagnosis within last
  • Individuals about to undergo a surgery or otherwise medical procedure that will
  • interfere with data collection and analyses planned within the current cohort,
  • will initially be excluded from participation, but are offered the opportunity
  • to participate at a later moment in time (e.g., after 3 months are myocardial
  • infarction patients are eligible for participation).
  • Additional inclusion criteria valid only for the other food additives and
  • limonene breath test
  • All those listed in the main protocol +
  • Inability to complete the breath sampling procedure
  • Known carrier of a-1 Antitrypsin deficiency

研究者

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